01973
Acide 4-aminobenzoïque
analytical standard
Synonyme(s) :
PABA, Vitamine Bx, Vitamine H1
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About This Item
Formule linéaire :
H2NC6H4CO2H
Numéro CAS:
Poids moléculaire :
137.14
Numéro Beilstein :
471605
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24
Produits recommandés
Qualité
analytical standard
Niveau de qualité
Pureté
≥98.0% (HPLC)
Durée de conservation
limited shelf life, expiry date on the label
Technique(s)
HPLC: suitable
gas chromatography (GC): suitable
Pf
186-188 °C
187-189 °C (lit.)
Densité
1.374 g/mL at 25 °C (lit.)
Application(s)
cleaning products
cosmetics
environmental
food and beverages
personal care
Format
neat
Chaîne SMILES
Nc1ccc(cc1)C(O)=O
InChI
1S/C7H7NO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,8H2,(H,9,10)
Clé InChI
ALYNCZNDIQEVRV-UHFFFAOYSA-N
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Application
- 4-Aminobenzoic Acid (PABA) in Pharmaceutical Development: Recognized as a valuable biochemical research reagent, 4-aminobenzoic acid is extensively used in the synthesis of various pharmaceutical compounds. Its role as a building block in drug design is crucial for developing new therapeutic agents, particularly in the fields of dermatology and oncology (Clegg and Nichol, 2024).
- UV Protection Research: PABA is renowned for its UV-absorbing properties, making it a key ingredient in sunscreen formulations. Ongoing research evaluates its efficacy and safety, ensuring optimal protection against UV radiation and its potential role in preventing skin cancer (Wang et al., 2024).
- Enzyme Inhibitor Studies: As a nucleoside enzyme inhibitor, 4-aminobenzoic acid is pivotal in biochemical studies that explore the inhibition mechanisms of specific enzymes. These studies are fundamental for understanding disease pathways and developing enzyme-targeted therapies (Buch et al., 2024).
- Vitamin B10 Research: Also known as Vitamin B10, PABA is studied for its role in human nutrition and its therapeutic effects, including in the management of fibrotic skin disorders and hair growth promotion. Research continues to uncover the broader health benefits of this compound (Berto et al., 2024).
- High-Purity PABA for Laboratory Applications: In scientific research, high-purity 4-aminobenzoic acid is essential for conducting precise and controlled experiments, particularly in studies related to its pharmacological properties and its interaction with other biochemical substances in the body (Park et al., 2024).
Conditionnement
Bottomless glass bottle. Contents are inside inserted fused cone.
Autres remarques
Ion Mobility: TWCCSN2 value of 133.2 Å2 [M+H]+
The collision cross section (CCS) measurement was provided by Waters Corporation, using the SYNAPT XS mass spectrometer.
For a description and overview of how ion mobility enables the measurement of the CCS of an ion visit ims.waters.com.
Further information on the SYNAPT XS mass spectrometer can be found on the IMS microsite and product webpage.
TWCCS measurements are expected to be within 2% of this reference value.
P/N 01973 is part of the Waters Extractables & Leachables UNIFI scientific library which can be downloaded from Waters Marketplace.
The collision cross section (CCS) measurement was provided by Waters Corporation, using the SYNAPT XS mass spectrometer.
For a description and overview of how ion mobility enables the measurement of the CCS of an ion visit ims.waters.com.
Further information on the SYNAPT XS mass spectrometer can be found on the IMS microsite and product webpage.
TWCCS measurements are expected to be within 2% of this reference value.
P/N 01973 is part of the Waters Extractables & Leachables UNIFI scientific library which can be downloaded from Waters Marketplace.
Mentions de danger
Conseils de prudence
Classification des risques
Aquatic Chronic 3
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 2
Point d'éclair (°F)
339.8 °F - closed cup
Point d'éclair (°C)
171 °C - closed cup
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A strategy based on negative ion electrospray ionization tandem mass spectrometry and closed-ring labeling with both 8-aminopyrene-1,3,6-trisulfonate (APTS) and p-aminobenzoic acid ethyl ester (ABEE) was developed for linkage and branch determination of high-mannose oligosaccharides. X-type cross-ring fragment ions obtained from
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Serum fluorescein and p-aminobenzoic acid were measured during a urine pancreolauryl and an N-benzoyl-l-tyrosyl-p-aminobenzoic acid (NBT-PABA) test in 22 healthy controls, 17 patients with gastrointestinal nonpancreatic diseases (normal secretin-pancreozymin test), and 31 patients with abnormal exocrine pancreatic function due to
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